nefazodone hydrochloride

Generic: nefazodone hydrochloride

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nefazodone hydrochloride
Generic Name nefazodone hydrochloride
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nefazodone hydrochloride 100 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-1024
Product ID 0093-1024_11cdc932-271c-4988-aad9-076340888bce
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076037
Listing Expiration 2026-12-31
Marketing Start 2003-09-16

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00931024
Hyphenated Format 0093-1024

Supplemental Identifiers

RxCUI
1098649 1098666 1098670 1098674 1098678
UPC
0300931024060 0300937113065
UNII
27X63J94GR

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name nefazodone hydrochloride (source: ndc)
Generic Name nefazodone hydrochloride (source: ndc)
Application Number ANDA076037 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (0093-1024-06)
source: ndc

Packages (1)

0093-1024-06 60 TABLET in 1 BOTTLE (0093-1024-06)

Ingredients (1)

nefazodone hydrochloride (100 mg/1)

Linked Drug Pages (1)

Nefazodone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "11cdc932-271c-4988-aad9-076340888bce", "openfda": {"upc": ["0300931024060", "0300937113065"], "unii": ["27X63J94GR"], "rxcui": ["1098649", "1098666", "1098670", "1098674", "1098678"], "spl_set_id": ["51ff7db5-aaf9-4c3c-86e6-958ebf16b60f"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (0093-1024-06)", "package_ndc": "0093-1024-06", "marketing_start_date": "20030916"}], "brand_name": "Nefazodone Hydrochloride", "product_id": "0093-1024_11cdc932-271c-4988-aad9-076340888bce", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "0093-1024", "generic_name": "Nefazodone Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nefazodone Hydrochloride", "active_ingredients": [{"name": "NEFAZODONE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA076037", "marketing_category": "ANDA", "marketing_start_date": "20030916", "listing_expiration_date": "20261231"}